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1.
Neurol Clin Pract ; 10(2): 170-177, 2020 Apr.
Article in English | MEDLINE | ID: mdl-32309036

ABSTRACT

PURPOSE OF REVIEW: Diverse adverse events have been associated with administration of glatiramer acetate (GA), mainly local reactions at the injection site. Other, less frequent generalized reactions include isolated postinjection reactions and anaphylaxis, which may lead to discontinuation of GA. RECENT FINDINGS: Close collaboration between the allergy and neurology departments is needed to study adverse reactions to GA. The allergy study should include a detailed history and skin prick and intradermal tests with GA and, if possible, determination of specific IgE levels. Furthermore, the implication of other drugs should be ruled out. SUMMARY: An accurate diagnosis of reactions to GA is essential if we are to confirm or rule out allergy to GA. When an allergy diagnosis is confirmed or firmly suspected based on clinical evidence, desensitization protocols are increasingly seen as safe methods for reintroduction of GA.

8.
J Allergy Clin Immunol ; 119(4): 960-4, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17292954

ABSTRACT

BACKGROUND: Because nonsteroidal anti-inflammatory drug (NSAID) intolerance depends on COX-1 inhibition, preferential or selective COX-2 inhibitors have been thought to be well tolerated by these patients. OBJECTIVE: The aim of this study is to evaluate tolerability to nabumetone and meloxicam in patients with NSAID intolerance. METHODS: Seventy patients intolerant to NSAIDs were selected. Thirty subjects were patients with asthma with respiratory (rhinitis-asthma) intolerance to NSAIDs (group A); 40 patients (group B) had cutaneous-mucous (urticaria-angioedema) NSAID intolerance. Diagnosis was based on clinical histories in all patients, and it was confirmed by positive single-blind placebo-controlled oral challenge test in 36 patients. After written informed consent, a single-blind placebo-controlled oral challenge test with nabumetone in all patients (2 g except for 11 patients who reached 1 g) and meloxicam (15 mg) in 51 patients was performed. RESULTS: Of the total selected, 94.3% tolerated 1 g nabumetone. In those who reached the 2-g dose, the tolerability was 83.6%. With respect to meloxicam, 96.1% of patients, tolerated 15 mg. No significant difference in nabumetone and meloxicam tolerability was observed between groups A and B. CONCLUSION: The results of this study confirm a high percentage of tolerability to the maximum therapeutic dosage of nabumetone and meloxicam in patients with NSAID intolerance, both in those with cutaneous/mucous manifestations and in those with respiratory disease. CLINICAL IMPLICATIONS: Nabumetone and meloxicam are safe alternatives in NSAID-intolerant patients.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Butanones/therapeutic use , Cyclooxygenase Inhibitors/therapeutic use , Drug Resistance, Multiple , Thiazines/therapeutic use , Thiazoles/therapeutic use , Adult , Aged , Angioedema/drug therapy , Angioedema/enzymology , Asthma/drug therapy , Asthma/enzymology , Butanones/adverse effects , Cyclooxygenase 1/metabolism , Cyclooxygenase 2 Inhibitors/therapeutic use , Cyclooxygenase Inhibitors/adverse effects , Drug Resistance, Multiple/immunology , Female , Humans , Male , Meloxicam , Middle Aged , Nabumetone , Rhinitis/drug therapy , Rhinitis/enzymology , Single-Blind Method , Thiazines/adverse effects , Thiazoles/adverse effects
10.
Am J Clin Dermatol ; 5(5): 351-5, 2004.
Article in English | MEDLINE | ID: mdl-15554736

ABSTRACT

INTRODUCTION: Sympathomimetic (alpha-adrenergic) drugs are mainly used because of their vasoconstrictor properties, for nasal congestion, or as mydriatics. Although sympathomimetic drugs are used often, allergic reactions are rare, especially when the drugs are administered systemically. Cross-reactivity may exist among catecholamine derivatives, although reported data on this are contradictory. In this study, we investigate if there is cross-reactivity in patch tests among these drugs. MATERIAL AND METHODS: Patch tests with 10% phenylephrine and 10% pseudoephedrine in petrolatum, and 10% and 20% ephedrine, 10% phenylpropanolamine, 5% fepradinol, 1% methoxamine, and 10% oxymetazoline, all administered in dimethyl sulfoxide (DMSO), were carried out in 14 patients with a history of allergy to any of these drugs. DMSO was used as the negative control. RESULTS: All patients except one (patient number five) showed positive patch-test reactions to at least two different drugs. Nine patients (64.3%) were cross-sensitized to three or more different drugs, and 57.1% of patients were sensitized to four or more sympathomimetic drugs. Patients who experienced generalized rashes caused by orally administered pseudoephedrine had a stronger response and more cross-reactivity with other sympathomimetic drugs in patch tests than those who experienced local contact dermatitis. CONCLUSIONS: We conclude that there is cross-reactivity among the different sympathomimetic drugs tested, especially if the drug is administered systemically.


Subject(s)
Allergens/immunology , Conjunctivitis, Allergic/immunology , Dermatitis, Allergic Contact/immunology , Mydriatics/immunology , Patch Tests , Sympathomimetics/immunology , Adult , Aged , Aged, 80 and over , Allergens/adverse effects , Cross Reactions , Dimethyl Sulfoxide , Ephedrine/immunology , Ethanolamines/immunology , Female , Humans , Male , Methoxamine/immunology , Middle Aged , Mydriatics/adverse effects , Oxymetazoline/immunology , Patch Tests/methods , Phenylephrine/immunology , Phenylpropanolamine/immunology , Single-Blind Method , Sympathomimetics/adverse effects , Time Factors
11.
Allergy Asthma Proc ; 24(4): 265-8, 2003.
Article in English | MEDLINE | ID: mdl-12974193

ABSTRACT

A 42-year-old woman reported immediate rhinoconjunctivitis, asthma, and contact urticaria while handling bird food. Skin-prick tests were positive to Lolium, Cynodon, Phragmites, Cupressus sempervirens, Cupressus arizonica, Chenopodium, sunflower pollen and seed, mugwort, chamomile, Chrysanthemum, Taraxacum, canary seed, and black seed (Guizotia abyssinica). The patient's serum-specific immunoglobulin (IgE) to Taraxacum, black seed, and canary seed was positive. Enzyme-linked immunosorbent assay inhibition studies revealed a 97 and 27% IgE-binding inhibition of whole canary food IgE by black seed and Taraxacum pollen, respectively. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis immunoblotting showed two IgE-binding protein bands of 11 and 44 kDa in the G. abyssinica extract. These two bands were totally inhibited by sunflower seed, mugwort, and Taraxacum extracts. Specific bronchial challenge with black seed extract was positive. The patient was able to feed her canary with birdseeds after she removed black seeds. We report a case of asthma caused by black seed (G. abyssinica) used as canary food in a patient previously allergic to pollen (olea europaea, grass, and mugwort) and sunflower seeds.


Subject(s)
Animal Feed/poisoning , Asthma/etiology , Adult , Asteraceae , Female , Humans , Seeds
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